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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936584Generated: November 3, 2026

5-Aminobenzimidazole → HCID 178507337, compound

https://huagongshe.com/reaction/1936584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-AminobenzimidazoleHCID 13623—
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
ProductHCID 178507337HCID 178507337—

Reaction Steps

To a solution of 1.08 g of 5-aminobenzimidazole in 20 mL of glacial acetic acid are added 2.68 g of sodium acetate. To this solution is added dropwise 0.4 mL of bromine. The resulting brown precipitate is stirred at room temperature for 2 hours. The reaction mixture is rotary evaporated and the residue is diluted with water and ethyl acetate. The mixture is basified with 1 N sodium hydroxide and decanted. The organic layer is washed with water followed by brine. The aqueous layers are extracted with ethyl acetate; the combined organic layers are dried over magnesium sulfate, filtered and rotary evaporated. The residue is purified by flash column chromatography on silica gel, eluting with 12.5 to 16.5% methanol/methylene chloride followed by recrystallization from hexanes/ethyl acetate to provide 887 mg of 5-amino-4-bromobenzimidazole as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391878B2
Source datasetuspto-grants-2002_05
ORD IDord-322ad2c7a534470ea03ee0c5fe81abf3
Source noteuspto-grants-2002_05